A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586597



Internal ID20959668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17131102..17131533hg38UCSC Ensembl
chr11:17152649..17153080hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232171
Samples
Known GenesPIK3C2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer